TW200505895A - Piperidyl- and piperazinyl-alkylcarbamate derivatives, preparation and therapeutic application thereof - Google Patents
Piperidyl- and piperazinyl-alkylcarbamate derivatives, preparation and therapeutic application thereofInfo
- Publication number
- TW200505895A TW200505895A TW093112818A TW93112818A TW200505895A TW 200505895 A TW200505895 A TW 200505895A TW 093112818 A TW093112818 A TW 093112818A TW 93112818 A TW93112818 A TW 93112818A TW 200505895 A TW200505895 A TW 200505895A
- Authority
- TW
- Taiwan
- Prior art keywords
- therapeutic application
- piperidyl
- piperazinyl
- preparation
- alkylcarbamate
- Prior art date
Links
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- C07D211/08—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members with hydrocarbon or substituted hydrocarbon radicals directly attached to ring carbon atoms
- C07D211/18—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members with hydrocarbon or substituted hydrocarbon radicals directly attached to ring carbon atoms with substituted hydrocarbon radicals attached to ring carbon atoms
- C07D211/26—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members with hydrocarbon or substituted hydrocarbon radicals directly attached to ring carbon atoms with substituted hydrocarbon radicals attached to ring carbon atoms with hydrocarbon radicals, substituted by nitrogen atoms
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- C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
- C07D471/04—Ortho-condensed systems
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- C07D—HETEROCYCLIC COMPOUNDS
- C07D491/00—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00
- C07D491/02—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00 in which the condensed system contains two hetero rings
- C07D491/04—Ortho-condensed systems
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D495/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms
- C07D495/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms in which the condensed system contains two hetero rings
- C07D495/04—Ortho-condensed systems
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Abstract
Compound corresponding to the general formula (I): , in which A = N or CR2; R2 = H, F, OH, CN, CF3, C1-g-alkyl or C1-6-alkoxy; n = 2 or 3 and m = 2 when A = N; n = 1, 2 or 3 and m = 1 or 2 when A = CR2 B = covalent bond or C1-8-alkylene; R1 = optionally substituted heteroaryl; R3 = CHR4CONHR5; P4 = H or C1-6-alkyl; R5 = H, C1-6-aikyl, C1-7-cycloalkyl or C3-7-cycloalkyl-C2-6-alkylene; in the form of the base, an acid-addition salt, a hydrate or a solvate. Therapeutic application.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
FR0305540A FR2854633B1 (en) | 2003-05-07 | 2003-05-07 | PIPERIDINYL-AND PIPERAZINYL-ALKYLCARBAMATES DERIVATIVES, THEIR PREPARATION AND THEIR THERAPEUTIC USE |
Publications (2)
Publication Number | Publication Date |
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TW200505895A true TW200505895A (en) | 2005-02-16 |
TWI337607B TWI337607B (en) | 2011-02-21 |
Family
ID=33306203
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
TW093112818A TWI337607B (en) | 2003-05-07 | 2004-05-06 | Piperidyl- and piperazinyl-alkylcarbamate derivatives, preparation and therapeutic application thereof |
Country Status (27)
Country | Link |
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US (3) | US7214798B2 (en) |
EP (1) | EP1633735B1 (en) |
JP (2) | JP4669836B2 (en) |
KR (1) | KR20060009900A (en) |
CN (2) | CN101712660A (en) |
AR (1) | AR044178A1 (en) |
AT (1) | ATE535518T1 (en) |
AU (1) | AU2004236006B2 (en) |
BR (1) | BRPI0410123A (en) |
CA (1) | CA2521700A1 (en) |
CO (1) | CO5640105A2 (en) |
EA (1) | EA009468B1 (en) |
FR (1) | FR2854633B1 (en) |
HK (1) | HK1093508A1 (en) |
IL (1) | IL171694A (en) |
IS (1) | IS8070A (en) |
MA (1) | MA27791A1 (en) |
ME (1) | MEP22308A (en) |
MX (1) | MXPA05011941A (en) |
NO (1) | NO20055204L (en) |
NZ (1) | NZ542941A (en) |
RS (1) | RS20050805A (en) |
TN (1) | TNSN05253A1 (en) |
TW (1) | TWI337607B (en) |
UA (1) | UA81808C2 (en) |
WO (1) | WO2004099176A1 (en) |
ZA (1) | ZA200508158B (en) |
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GB2397067B (en) * | 2002-12-23 | 2005-05-11 | Destiny Pharma Ltd | Porphin & azaporphin derivatives with at least one cationic-nitrogen-containing meso-substituent for use in photodynamic therapy & in vitro sterilisation |
FR2864080B1 (en) | 2003-12-23 | 2006-02-03 | Sanofi Synthelabo | 1-PIPERAZINE-AND-1-HOMOPIPERAZINE-CARBOXYLATE DERIVATIVES, THEIR PREPARATION AND THEIR THERAPEUTIC USE |
FR2866888B1 (en) | 2004-02-26 | 2006-05-05 | Sanofi Synthelabo | ALKYLPIPERAZINE- AND ALKYLHOMOPIPERAZINE-CARBOXYLATE DERIVATIVES, THEIR PREPARATION AND THEIR THERAPEUTIC USE |
FR2866885B1 (en) * | 2004-02-26 | 2007-08-31 | Sanofi Synthelabo | PIPERIDINYLALKYLCARBAMATES DERIVATIVES, THEIR PREPARATION AND THERAPEUTIC USE THEREOF |
FR2866884B1 (en) * | 2004-02-26 | 2007-08-31 | Sanofi Synthelabo | ARYL-AND HETEROARYL-PIPERIDINECARBOXYLATE DERIVATIVES, THEIR PREPARATION AND THEIR THERAPEUTIC USE |
FR2866886B1 (en) * | 2004-02-26 | 2007-08-31 | Sanofi Synthelabo | ARYL-AND HETEROARYL-AKYLCARBAMATES DERIVATIVES, THEIR PREPARATION AND THEIR THERAPEUTIC USE |
GB2415372A (en) | 2004-06-23 | 2005-12-28 | Destiny Pharma Ltd | Non photodynamical or sonodynamical antimicrobial use of porphyrins and azaporphyrins containing at least one cationic-nitrogen-containing substituent |
TW200633990A (en) | 2004-11-18 | 2006-10-01 | Takeda Pharmaceuticals Co | Amide compound |
US7598249B2 (en) * | 2004-12-30 | 2009-10-06 | Janssen Pharmaceutica N.V. | Piperazinyl and piperidinyl ureas as modulators of fatty acid amide hydrolase |
FR2885364B1 (en) * | 2005-05-03 | 2007-06-29 | Sanofi Aventis Sa | ALKYL-, ALKENYL- AND ALKYNYLCARBAMATES DERIVATIVES, THEIR PREPARATION AND THEIR THERAPEUTIC APPLICATION |
PE20070099A1 (en) * | 2005-06-30 | 2007-02-06 | Janssen Pharmaceutica Nv | N-HETEROARYLPIPERAZINYL UREAS AS MODULATORS OF FATTY ACID AMIDE HYDROLASE |
EP1903037A1 (en) * | 2006-09-07 | 2008-03-26 | Bayer Schering Pharma Aktiengesellschaft | 1-(hetero)aryl-3-[heteroaryl-piperidin-4yl]-thiourea derivatives as modulators of EP2 receptors |
WO2008030752A2 (en) * | 2006-09-07 | 2008-03-13 | N.V. Organon | Methods for determining effective doses of fatty acid amide hydrolase inhibitors in vivo |
WO2008042892A2 (en) * | 2006-10-02 | 2008-04-10 | N.V. Organon | Fatty acid amide hydrolase inhibitors for energy metabolism disorders |
EP2096915A1 (en) * | 2006-11-20 | 2009-09-09 | N.V. Organon | Metabolically-stabilized inhibitors of fatty acid amide hydrolase |
TWI434842B (en) * | 2008-07-14 | 2014-04-21 | Astellas Pharma Inc | Azole compounds |
FR2934265B1 (en) * | 2008-07-23 | 2010-07-30 | Sanofi Aventis | ALKYLTHIAZOLE CARBAMATE DERIVATIVES, THEIR PREPARATION AND THEIR THERAPEUTIC APPLICATION |
FR2938537B1 (en) * | 2008-11-14 | 2012-10-26 | Sanofi Aventis | ALKYL-HETEROCYCLE CARBAMATE DERIVATIVES, THEIR PREPARATION AND THERAPEUTIC USE THEREOF |
FR2941696B1 (en) * | 2009-02-05 | 2011-04-15 | Sanofi Aventis | AZASPIRANYL-ALKYLCARBAMATES DERIVATIVES OF 5-CHAIN HETEROCYCLES, THEIR PREPARATION AND THEIR THERAPEUTIC USE |
CN102459240A (en) * | 2009-04-22 | 2012-05-16 | 詹森药业有限公司 | Azetidinyl diamides as monoacylglycerol lipase inhibitors |
FR2945531A1 (en) * | 2009-05-12 | 2010-11-19 | Sanofi Aventis | 7-AZA-SPIRO® 3,5-NONANE-7-CARBOXYLATE DERIVATIVES, THEIR PREPARATION AND THEIR THERAPEUTIC APPLICATION |
EP2477981A1 (en) * | 2009-09-14 | 2012-07-25 | Recordati Ireland Limited | Heterocyclic mglu5 antagonists |
US20130150346A1 (en) | 2010-01-08 | 2013-06-13 | Quest Ventures Ltd. | Use of FAAH Inhibitors for Treating Parkinson's Disease and Restless Legs Syndrome |
US20130224151A1 (en) | 2010-03-31 | 2013-08-29 | United States Of America | Use of FAAH Inhibitors for Treating Abdominal, Visceral and Pelvic Pain |
UA108233C2 (en) | 2010-05-03 | 2015-04-10 | Fatty acid amide hydrolysis activity modulators | |
GB201017345D0 (en) | 2010-10-14 | 2010-11-24 | Proximagen Ltd | Receptor antagonists |
CN107982266B (en) * | 2012-01-06 | 2021-07-30 | H.隆德贝克有限公司 | Carbamate compounds and methods of making and using the same |
DE102012018115A1 (en) | 2012-09-13 | 2014-03-13 | Matthias Lehr | New aryl-N-(arylalkyl) carbamate compounds, used to prepare pharmaceutical composition for prophylactic and/or therapeutic treatment of diseases including e.g. acute and chronic neurogenic pain, and neurological and psychiatric diseases |
RU2693457C2 (en) * | 2013-07-18 | 2019-07-03 | Фондацьоне Иституто Итальяно Ди Текнолоджия | Phenylcarbamates and use thereof as enzyme inhibitors of hydrolases of fatty acid amides (faah) and dopamine receptor d3 (d3dr) modulators |
DE102013016573A1 (en) | 2013-10-04 | 2015-04-09 | Matthias Lehr | 1-Tetrazolylpropan-2-ones as inhibitors of cytosolic phospholipase A2 and fatty acid amide hydrolase, in particular suitable for topical application |
EP3277284B1 (en) | 2015-04-02 | 2020-08-05 | Proximagen, Llc | Novel therapies for cancer |
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Publication number | Priority date | Publication date | Assignee | Title |
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DE3235565A1 (en) * | 1982-09-25 | 1984-03-29 | Boehringer Ingelheim KG, 6507 Ingelheim | PIPERIDE DERIVATIVES, THEIR PRODUCTION AND USE |
FR2761266B1 (en) * | 1997-03-28 | 1999-07-02 | Sanofi Sa | PHARMACEUTICAL COMPOSITION FORMED BY WET GRANULATION FOR THE ORAL ADMINISTRATION OF A DERIVATIVE OF N-PIPERIDINO-3- PYRAZOLECARBOXAMIDE, ITS SALTS AND THEIR SOLVATES |
FR2783246B1 (en) * | 1998-09-11 | 2000-11-17 | Aventis Pharma Sa | AZETIDINE DERIVATIVES, THEIR PREPARATION AND THE MEDICINES CONTAINING THEM |
FR2805818B1 (en) * | 2000-03-03 | 2002-04-26 | Aventis Pharma Sa | AZETIDINE DERIVATIVES, THEIR PREPARATION AND THE PHARMACEUTICAL COMPOSITIONS CONTAINING THEM |
FR2816938B1 (en) | 2000-11-22 | 2003-01-03 | Sanofi Synthelabo | 3-AROYLINDOLE DERIVATIVES, PROCESS FOR THEIR PREPARATION AND PHARMACEUTICAL COMPOSITIONS CONTAINING THEM |
FR2843964B1 (en) * | 2002-08-29 | 2004-10-01 | Sanofi Synthelabo | DIOXANE-2-ALKYLCARBAMATES DERIVATIVES, THEIR PREPARATION AND THEIR THERAPEUTIC APPLICATION |
-
2003
- 2003-05-07 FR FR0305540A patent/FR2854633B1/en not_active Expired - Fee Related
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2004
- 2004-05-06 MX MXPA05011941A patent/MXPA05011941A/en active IP Right Grant
- 2004-05-06 TW TW093112818A patent/TWI337607B/en not_active IP Right Cessation
- 2004-05-06 EP EP04742661A patent/EP1633735B1/en not_active Expired - Lifetime
- 2004-05-06 ZA ZA200508158A patent/ZA200508158B/en unknown
- 2004-05-06 JP JP2006505833A patent/JP4669836B2/en not_active Expired - Fee Related
- 2004-05-06 ME MEP-223/08A patent/MEP22308A/en unknown
- 2004-05-06 NZ NZ542941A patent/NZ542941A/en not_active IP Right Cessation
- 2004-05-06 AU AU2004236006A patent/AU2004236006B2/en not_active Ceased
- 2004-05-06 KR KR1020057021049A patent/KR20060009900A/en active IP Right Grant
- 2004-05-06 CN CN200910247187A patent/CN101712660A/en active Pending
- 2004-05-06 CN CN2004800183223A patent/CN1812980B/en not_active Expired - Fee Related
- 2004-05-06 AT AT04742661T patent/ATE535518T1/en active
- 2004-05-06 AR ARP040101538A patent/AR044178A1/en unknown
- 2004-05-06 EA EA200501477A patent/EA009468B1/en not_active IP Right Cessation
- 2004-05-06 BR BRPI0410123-5A patent/BRPI0410123A/en not_active IP Right Cessation
- 2004-05-06 RS YUP-2005/0805A patent/RS20050805A/en unknown
- 2004-05-06 WO PCT/FR2004/001102 patent/WO2004099176A1/en active Application Filing
- 2004-05-06 CA CA002521700A patent/CA2521700A1/en not_active Abandoned
- 2004-06-05 UA UAA200511617A patent/UA81808C2/en unknown
-
2005
- 2005-10-06 TN TNP2005000253A patent/TNSN05253A1/en unknown
- 2005-10-13 IS IS8070A patent/IS8070A/en unknown
- 2005-10-28 CO CO05110295A patent/CO5640105A2/en not_active Application Discontinuation
- 2005-10-28 US US11/262,211 patent/US7214798B2/en not_active Expired - Fee Related
- 2005-10-31 IL IL171694A patent/IL171694A/en not_active IP Right Cessation
- 2005-11-02 MA MA28577A patent/MA27791A1/en unknown
- 2005-11-04 NO NO20055204A patent/NO20055204L/en not_active Application Discontinuation
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2007
- 2007-01-16 HK HK07100548.0A patent/HK1093508A1/en not_active IP Right Cessation
- 2007-02-02 US US11/670,690 patent/US8034818B2/en not_active Expired - Fee Related
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2010
- 2010-11-26 JP JP2010264051A patent/JP2011063620A/en not_active Withdrawn
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2011
- 2011-09-09 US US13/229,106 patent/US20120004207A1/en not_active Abandoned
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